EP4282458A2 - System zur befeuchtung von medizinischen gasen - Google Patents

System zur befeuchtung von medizinischen gasen Download PDF

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Publication number
EP4282458A2
EP4282458A2 EP23189049.2A EP23189049A EP4282458A2 EP 4282458 A2 EP4282458 A2 EP 4282458A2 EP 23189049 A EP23189049 A EP 23189049A EP 4282458 A2 EP4282458 A2 EP 4282458A2
Authority
EP
European Patent Office
Prior art keywords
gases
housing
mask frame
liquid
humidifier
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP23189049.2A
Other languages
English (en)
French (fr)
Other versions
EP4282458A9 (de
EP4282458A3 (de
Inventor
Richard John Boyes
Christian Francis FISCHER
Charlotte Grace LAUS
Elmo Benson Stoks
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fisher and Paykel Healthcare Ltd
Original Assignee
Fisher and Paykel Healthcare Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fisher and Paykel Healthcare Ltd filed Critical Fisher and Paykel Healthcare Ltd
Publication of EP4282458A2 publication Critical patent/EP4282458A2/de
Publication of EP4282458A9 publication Critical patent/EP4282458A9/de
Publication of EP4282458A3 publication Critical patent/EP4282458A3/de
Pending legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10—Preparation of respiratory gases or vapours
    • A61M16/14—Preparation of respiratory gases or vapours by mixing different fluids, one of them being in a liquid phase
    • A61M16/16—Devices to humidify the respiration air
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M13/00—Insufflators for therapeutic or disinfectant purposes, i.e. devices for blowing a gas, powder or vapour into the body
    • A61M13/003—Blowing gases other than for carrying powders, e.g. for inflating, dilating or rinsing
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10—Preparation of respiratory gases or vapours
    • A61M16/1075—Preparation of respiratory gases or vapours by influencing the temperature
    • A61M16/109—Preparation of respiratory gases or vapours by influencing the temperature the humidifying liquid or the beneficial agent
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10—Preparation of respiratory gases or vapours
    • A61M16/1075—Preparation of respiratory gases or vapours by influencing the temperature
    • A61M16/1095—Preparation of respiratory gases or vapours by influencing the temperature in the connecting tubes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10—Preparation of respiratory gases or vapours
    • A61M16/14—Preparation of respiratory gases or vapours by mixing different fluids, one of them being in a liquid phase
    • A61M16/142—Preparation of respiratory gases or vapours by mixing different fluids, one of them being in a liquid phase with semi-permeable walls separating the liquid from the respiratory gas
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/36—General characteristics of the apparatus related to heating or cooling
    • A61M2205/3653—General characteristics of the apparatus related to heating or cooling by Joule effect, i.e. electric resistance
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/75—General characteristics of the apparatus with filters
    • A61M2205/7536—General characteristics of the apparatus with filters allowing gas passage, but preventing liquid passage, e.g. liquophobic, hydrophobic, water-repellent membranes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2206/00—Characteristics of a physical parameter; associated device therefor
    • A61M2206/10—Flow characteristics
    • A61M2206/12—Flow characteristics the flow being spirally in a plane, e.g. against a plane side of a membrane filter element

Definitions

  • the present disclosure generally relates to a system for the humidification of medical gases. More particularly, the present disclosure relates to a system for the humidification of medical gases using an inline humidifier.
  • a humidification apparatus can be used to provide heated and humidified gases to a patient via a patient interface for various purposes, including respiratory therapy and laparoscopic procedures.
  • humidified medical gases help protect the peritoneum from desiccation and inflammation that can be caused by cold dry gases used during surgical procedures.
  • Pass-over humidification devices supply heated, humidified gases to a patient.
  • Such humidification systems typically comprise a humidification apparatus, a humidification chamber, a tube system, and a patient interface.
  • the humidification apparatus comprises a heater plate that is configured to heat the humidification chamber. This causes vapour to form, which enters a flow of gases flowing through the humidification chamber, humidifying the medical gases.
  • Such humidification systems can have a large footprint and require large volumes of liquid for humidification to take place. Heat is applied to the heater plate of the humidification chamber to form vapour, meaning the heater plate is hot to touch.
  • Humidification systems for surgical applications may comprise a tube with a wicking or absorptive material positioned within the gases flow path.
  • the wicking or absorptive material connects with an external liquid supply or reservoir, and liquid travels along the wick to the gases flow path, for example, via capillary action. Heat is applied to the wicking material, releasing vapour into the gases flow path in the tube.
  • Some humidification systems hold liquid within compartments or reservoirs within the tube. Heat is applied to the liquid to form vapour, and the vapour moves through a permeable membrane into the lumen of the tube.
  • An external liquid supply reduces the portability of the humidification system, increases the number of set-up steps, and thus increases the overall complexity of the system.
  • a system with an external liquid supply also typically requires a large portion of the limited space within a surgical theatre.
  • Liquid held in reservoirs within the tube increases the weight and reduces the flexibility of the tube, thereby making the tube difficult to manipulate within the surgical space.
  • a humidifier comprising an inlet and an outlet and a gases flow path extending from the inlet to the outlet; a liquid reservoir; in thermal communication with; or configured to be in thermal communication with in use, a heater; and a permeable wall separating the liquid reservoir from the gases flow path; wherein, in use, the heater heats liquid stored in the liquid reservoir to form vapour, and the vapour passes through the permeable wall to humidify gases in the gases flow path.
  • the reservoir is preferably configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidifier.
  • the gases flow path is preferably defined, at least in part, by a spirally wound wall within the housing.
  • the humidifier may comprise a hydrophobic housing.
  • the humidifier preferably comprises a tape. More preferably, the permeable wall comprises a tape.
  • the tape preferably comprises a hydrophilic material.
  • the heater may include one or more heater wires or elements and may be provided inside the humidifier (i.e. in close proximity to the reservoir) or adjacent a surface thereof, such as the base.
  • the humidifier may be configured to thermally couple with a heater so as to receive heat from another source.
  • a more conventional humidifier heater arrangement could be used where the humidifier is adapted to sit on and/or abut a heater plate.
  • walls of high thermal conductivity are provided to facilitate heat transfer to the reservoir. Such walls or parts thereof may, for example, be formed from a metal such as aluminium.
  • a humidifier comprising a housing having an inlet and an outlet; and a tape disposed within the housing and at least partially defining a gases flow path through the housing between the inlet and the outlet, wherein the tape comprises a hydrophilic material configured to hold a volume of liquid and a heating mechanism configured to heat liquid held within the hydrophilic material to produce vapour.
  • the hydrophilic material is preferably configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidifier.
  • the hydrophilic material may be configured to be pre-loaded prior to use to cause liquid to be held within the hydrophilic material.
  • the tape may be spirally wound within the housing.
  • the housing may comprise a hydrophobic material.
  • the heating mechanism preferably comprises at least one heater wire disposed within and surrounded by the hydrophilic material.
  • the heating mechanism preferably comprises at least one heater wire disposed within and surrounded by the hydrophilic material.
  • other heating arrangements are possible in the same manner as stated in respect of the first aspect.
  • the invention also provides a humidification system comprising the humidifier of the first aspect and/or the second aspect.
  • the wall comprises a tape and/or a tape is positioned adjacent or affixed to the wall.
  • the humidification system preferably comprises a delivery tube coupled to the outlet and configured to, at least in part, transport gases from the housing to a patient in use.
  • a humidification system comprising a humidifier comprising an inlet and an outlet and a gases flow path extending from the inlet to the outlet; a liquid reservoir; a heater in thermal communication with the liquid reservoir; and a permeable wall separating the liquid reservoir from the gases flow path; wherein in use, the heater heats liquid stored in the liquid reservoir to form vapor, and the vapor passes through the permeable wall to humidify gases in the gases flow path; and a delivery tube coupled to the outlet and configured to transport gases from the housing to a patient in use.
  • the liquid reservoir may be configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidification system.
  • the gases flow path may be defined by a spirally wound wall within the housing.
  • the humidifier may comprise a hydrophobic housing.
  • the delivery tube may comprises a second heating mechanism.
  • the second heating mechanism may comprise at least one heater wire disposed within the delivery tube.
  • a humidification system comprising a humidifier comprising a housing having an inlet and an outlet; and a tape disposed within the housing and at least partially defining a gases flow path through the housing between the inlet and the outlet, wherein the tape comprises a hydrophilic material configured to hold a volume of liquid and a heating mechanism configured to heat liquid held within the hydrophilic material to produce vapour; and a delivery tube coupled to the outlet and configured to transport gases from the housing to a patient in use.
  • the hydrophilic material may be configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidification system.
  • the hydrophilic material may be configured to be pre-loaded prior to use to cause liquid to be held within the hydrophilic material.
  • the tape may be spirally wound within the housing.
  • the housing may comprise a hydrophobic material.
  • the heating mechanism may comprise at least one heater wire disposed within and surrounded by the hydrophilic material.
  • the delivery tube may comprise a second heating mechanism.
  • the second heating mechanism may comprise at least one heater wire disposed within the delivery tube.
  • a humidification system comprises an inline (i.e., in line with a delivery tube or conduit) humidifier to provide heated and humidified gases to a patient.
  • the humidification system advantageously requires reduced or minimal set-up steps due to the inline humidifier design. For example, there is no need for an external liquid reservoir to supply the system with sufficient liquid for the surgical procedure. Similarly, there is no need for a wick to convey liquid into the tube so that humidification can take place.
  • the inline humidifier and tube are not dependent on a specific orientation for functionality, which gives the medical practitioner more freedom to manipulate the system.
  • a humidification system includes a humidifier and a delivery tube.
  • the humidifier includes a housing having an inlet and an outlet and a tape disposed within the housing.
  • the tape at least partially defines a gases flow path through the housing between the inlet and the outlet.
  • the tape can include a hydrophilic or hygroscopic material configured to hold a volume of liquid and a heating mechanism to heat liquid held within the hydrophilic or hygroscopic material to produce vapour.
  • the delivery tube is coupled to the outlet and is configured to transport gases from the housing to a patient in use.
  • the hydrophilic or hygroscopic material is configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidification system. In some embodiments, the hydrophilic or hygroscopic material is configured to be pre-loaded prior to use to cause liquid to be held within the material. In some embodiments, the tape is spirally wound within the housing. In some embodiments, the housing comprises a hydrophobic material. In some embodiments, the heating mechanism comprises at least one heater wire disposed within and surrounded by the hydrophilic or hygroscopic material. The delivery tube can include a second heating mechanism. In some embodiments, the second heating mechanism comprises at least one heater wire disposed within the delivery tube.
  • a humidifier in some embodiments, includes a housing having an inlet and an outlet and a tape disposed within the housing.
  • the tape at least partially defines a gases flow path through the housing between the inlet and the outlet.
  • the tape includes a hydrophilic or hygroscopic material configured to hold a volume of liquid and a heating mechanism configured to heat liquid held within the hydrophilic material to produce vapour.
  • the hydrophilic or hygroscopic material is configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidification system.
  • the hydrophilic or hygroscopic material is configured to be pre-loaded prior to use to cause liquid to be held within the material.
  • the tape is spirally wound within the housing.
  • the housing comprises a hydrophobic material.
  • the heating mechanism comprises at least one heater wire disposed within and surrounded by the hydrophilic or hygroscopic material.
  • a humidification system includes a humidifier and a delivery tube.
  • the humidifier includes an inlet, an outlet, a gases flow path extending from the inlet to the outlet, a liquid reservoir, a heater in thermal communication with the liquid reservoir, and a permeable wall separating the liquid reservoir from the gases flow path.
  • the heater heats liquid stored in the liquid reservoir to form vapor, and the vapor passes through the permeable wall to humidify gases in the gases flow path.
  • the delivery tube is coupled to the outlet and configured to transport gases from the housing to a patient in use.
  • the liquid reservoir is configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidification system.
  • the gases flow path is defined by a spirally wound wall within the housing.
  • the humidifier comprises a hydrophobic housing.
  • the delivery tube can include a second heating mechanism.
  • the second heating mechanism comprises at least one heater wire disposed within the delivery tube.
  • an inline humidifier includes an inlet, an outlet, a gases flow path extending from the inlet to the outlet, a liquid reservoir, a heater in thermal communication with the liquid reservoir, and a permeable wall separating the liquid reservoir from the gases flow path.
  • the heater heats liquid stored in the liquid reservoir to form vapor, and the vapor passes through the permeable wall to humidify gases in the gases flow path.
  • the liquid reservoir is configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidification system.
  • the gases flow path is defined by a spirally wound wall within the housing.
  • the humidifier comprises a hydrophobic housing.
  • FIG. 1 illustrates a prior art humidification system 100 that is configured to deliver heated and humidified gases to a patient 101.
  • the humidification system 100 comprises a humidification apparatus 103, a humidification chamber 105, and a gases source 110.
  • the gases source 110 is an insufflator.
  • the humidification chamber 105 is configured to hold a volume of liquid, such as water.
  • the humidification apparatus 103 comprises a heating mechanism configured to heat the water within the humidification chamber 105 to form water vapour. Gases from the gases source 110 are heated and humidified as they pass through the humidification chamber 105, and the conditioned gases are delivered to the patient 101.
  • Gases as herein described refers to respiratory gases (for example, oxygen, air, nitrogen, carbon dioxide, or a combination of any of these), or surgical gases, (for example, carbon dioxide, nitrous, oxygen, air, helium, or a mixture of carbon dioxide with nitrous or oxygen).
  • respiratory gases for example, oxygen, air, nitrogen, carbon dioxide, or a combination of any of these
  • surgical gases for example, carbon dioxide, nitrous, oxygen, air, helium, or a mixture of carbon dioxide with nitrous or oxygen.
  • Other gases or combinations of gases also fall within the scope of the disclosed apparatus and systems.
  • FIG. 2 illustrates a prior art humidification system 200 that is configured to deliver heated and humidified gases to a patient 201.
  • the humidification system 200 comprises a tube humidifier 205, a water channel 207, a water supply 209, and a gases source 210.
  • the gases source 210 is an insufflator. Gases from the gases source 210 are delivered to the patient 201 via the tube humidifier 205.
  • the tube humidifier 205 comprises a wicking membrane that wicks water via the water channel 207 from the water supply 209. The wicked water is heated using a heating mechanism, thereby causing evaporation of the water.
  • the water vapour generated enters the lumen of the tube humidifier 205, thereby causing the gases flowing therein to become humidified.
  • the humidified gases are delivered to the patient 201.
  • humidification systems such as the system 100 and the system 200 require external liquid supplies (such as liquid supplies in the humidification chamber 105 or the water supply 209), which can decrease the portability and maneuverability of the system, increase the number of set-up steps, and increase the footprint of the system.
  • external liquid supplies such as liquid supplies in the humidification chamber 105 or the water supply 209
  • FIG. 3 illustrates a side or longitudinal cross-sectional view of an example embodiment of a humidification system 1100 including an inline humidifier 1102 according to the present disclosure.
  • the humidification system 1100 includes the inline humidifier 1102 and a delivery tube or conduit 1130.
  • the inline humidifier 1102 includes a housing 1110, a tape 1120, and one or more heating elements 1140.
  • the housing 1110 has a gases inlet 1112 and a gases outlet 1114.
  • the gases outlet 1114 is coupled to a first end of the delivery tube 1130 in use.
  • the delivery tube 1130 is permanently coupled to the gases outlet 1114.
  • the delivery tube 1130 can be removably coupled to the gases outlet 1114.
  • the delivery tube 1130 can be provided preassembled to the gases outlet 1114.
  • An opposite, second end 1134 of the delivery tube 1130 can be coupled to a patient interface, for example, a laparoscopic cannula, or another humidification system component in use.
  • the humidification system 1100 is disposable. In other embodiments, the humidification system 1100 can be refillable and/or sterilisable for reuse.
  • the housing 1110 can be made of a hydrophobic or any other gases and/or water impermeable or low permeability material.
  • the housing 1110 includes insulation to reduce or minimize heat transfer with the external environment or atmosphere.
  • the housing 1110 is generally disc-shaped or circular. However, other shapes are also possible, for example, quadrilateral, square, trapezoidal, parallelogram, or other shapes.
  • the gases inlet 1112 is disposed on a front side or face of the housing 1110, and the gases outlet 1114 is disposed on an opposite rear side or face of the housing 1110.
  • the gases inlet 1112 can be disposed on a rear side of the housing 1110 or on a side or edge of the housing 1110 and/or the gases outlet 1114 can be disposed on a front side of the housing 1110 or on a side or edge of the housing 1110.
  • the gases inlet 1112 can be positioned proximate an outer perimeter of the front side of the housing 1110 or closer to the outer perimeter than a center of the front side of the housing 1110.
  • the gases outlet 1114 can be positioned at or proximate a center of the rear side of the housing 1110.
  • the gases inlet 1112 can be positioned proximate the center of the housing 1110 and the gases outlet 1114 can be positioned proximate the outer perimeter of the housing 1110
  • both the gases inlet 1112 and the gases outlet 1114 can be positioned proximate the center of the housing 1110
  • both the gases inlet 1112 and the gases outlet 1114 can be positioned proximate the outer perimeter of the housing 1110
  • the gases inlet 1112 and the gases outlet 1114 can be positioned at any position between the center and outer perimeter on either side of the housing 1110.
  • the tape 1120 can include or be made of a hydrophilic or hygroscopic material that can absorb and/or retain a volume of liquid, such as water.
  • a hygroscopic material attracts and holds water molecules via adsorption.
  • a hygroscopic material can be porous, for example, like silica gel or zeolite, and/or can have surface features to increase the effective area of the material.
  • a hydrophilic material absorbs water in a vapor and/or liquid state.
  • a hydrophilic material can be foamed and/or can include surface features to increase the effective area of the material.
  • the tape 1120 can be made of Arnitel or another hydrophilic material.
  • the tape 1120 can include the heating elements 1140.
  • the heating elements 1140 can be placed within, on, or surrounding the tape 1120.
  • the heating elements 1140 of the tape 1120 include two heater wires disposed within and surrounded by the hydrophilic or hygroscopic material. In use, heat from the heating elements 1140 causes vapor to be released from the hydrophilic or hygroscopic material of the tape 1120.
  • the tape 1120 is disposed within the housing 1110 and arranged to define a gases flow path 1116 within the housing 1110 between the gases inlet 1112 and the gases outlet 1114.
  • the tape 1120 can be spirally wound within the housing 1110 as shown. Other arrangements for the tape 1120 within the housing 1110 are also possible.
  • a configuration or arrangement of the tape 1120 that creates a convoluted embodiment of the gases flow path 1116 can increase the degree or level of water vapor exchange as described in greater detail herein.
  • extrusions of a hydrophilic or hygroscopic material are arranged in a random, tangled manner in the housing 1110, similar to a bird nest.
  • Gases can flow freely through spaces between the extrusions of hydrophilic or hygroscopic material from the gases inlet 1112 to the gases outlet 1114.
  • the hydrophilic or hygroscopic material can be heated by a heater plate or one or more heater wires disposed within the housing 1110.
  • the tape 1120 can be arranged to form a 3D spiral arrangement of the gases flow path 1116, similar to a corkscrew.
  • the housing 1110 can include an internal liquid reservoir within the internal volume of the corkscrew.
  • the gases inlet 1112 is positioned proximate the outer perimeter of the housing 1110, and the gases outlet 1114 is positioned proximate the center of the housing 1110-- the gases flow path 1116 follows a spiral path from an outer perimeter of the housing 1110 to a center of the housing 1110.
  • gases in the gases flow path 1116 warm as the gases travel inward toward the center of the housing 1110 and to the gases outlet 1114, and the gases are insulated by gases in portions of the gases flow path 1116 disposed concentrically outward.
  • the gases flow path 1116 instead followed a path from the center of the housing 1110 to the perimeter of the housing 1110, the warmest gases at the end of the gases flow path 1116 and at the gases outlet 1114 would be at the outer perimeter of the housing 1110 and therefore less insulated, which could reduce the efficiency of the system.
  • a spiral arrangement of the gases flow path 1116 can advantageously reduce or minimize flow dead spots in which the flow of gases recirculates or slows.
  • the tape 1120 can be retained within the housing 1110 and/or retained in the spiral or other arrangement by clips or other retainers 1160, as shown in Figure 4 .
  • the humidification system 1100 or the humidifier 1102 can be supplied sterilized and ready for use.
  • the humidification system 1100 specifically the tape 1120, can be preloaded (e.g., during manufacturing and assembly or set-up) with a volume of liquid, such as water (e.g., in liquid form in a hygroscopic material or in liquid and/or vapor form in a hydrophilic material) prior to a surgical procedure or other use.
  • the tape 1120 can hold approximately 30% weight in water after a soak time of one hour.
  • the tape 1120 can be pre-soaked with a known and desired quantity of liquid, which can be calculated based on the average duration of a typical procedure for which the humidification system 1100 is intended to be used.
  • the humidification system 1100 therefore does not require a separate liquid reservoir or delivery system, and medical personnel need not input liquid into the system prior to use during set-up.
  • the humidifier 1102 can be refilled after use for re-use or during use if needed.
  • gases enter the housing 1110 through the gases inlet 1112, flow through the gases flow path 1116, exit the housing 1110 through the gases outlet 1114, flow through the delivery tube 1130, and are delivered to a patient, patient interface connector, or other humidification system component at the second end 1134.
  • Power is supplied to the heating elements 1140 such that the heating elements 1140 heat the liquid or vapor stored within the tape 1120 to release vapor into the gases flow path 1116. Gases flowing through the gases flow path 1116 are therefore humidified by the vapor released from the tape 1120.
  • the heated vapor can also heat the gases flowing through the gases flow path 1116.
  • the heating elements 1140 can also directly heat the gases flowing through the gases flow path 1116.
  • the configuration of the heating elements 1140 can affect the conditions of the gases exiting the gases flow path 1116.
  • the size and type of the heating elements 1140 can be determined based on the geometry of the tape 1120 and how the geometry affects the humidification of heated gases.
  • the hydrophobic, impermeable, or low permeability material of the housing 1110 can help hold the vapor within the housing 1110 to prevent or inhibit the vapor from being released through the housing 1110 to the atmosphere.
  • the tape 1120 can be an extruded polymer.
  • a cross-sectional shape of the tape 1120 can be selected to optimize various factors, for example, to increase or maximize the surface area of the tape 1120 exposed to the gases flow path 1116 to increase the level of vapor exchange into gases in the gases flow path 1116.
  • the cross-sectional shape of the tape 1120 is rectangular or generally rectangular. In other embodiments, the tape 1120 has an elliptical or other cross-sectional shape.
  • Figure 6A illustrates a cross-sectional view of a tape 1120a, an embodiment of the tape 1120 as used in the embodiment of Figures 3-5 .
  • the hydrophilic or hygroscopic material of the tape 1120a has been pre-soaked with liquid such as water.
  • Figures 6B-6C illustrate schematic cross-sectional views of a tape 1120b and a tape 1120c, which are alternative embodiments of the tape 1120.
  • the tape 1120b of Figure 6B includes an internal liquid reservoir or cavity 1122 within the hydrophilic or hygroscopic material of the tape 1120b.
  • the hydrophilic or hygroscopic material might not be pre-soaked. Instead, in use, heat from the heating elements 1140 causes the liquid within the reservoir 1122 to vaporize, and the vapor permeates through the hydrophilic or hygroscopic material of the tape 1120b into the gases flow path 1116.
  • the liquid reservoir 1122 may be able to be filled more quickly than the hydrophilic or hygroscopic material of the tape 1120b can absorb liquid via pre-soaking. The liquid reservoir 1122 may therefore reduce manufacturing or assembly time.
  • the tape 1120b can include the internal reservoir 1122 and the hydrophilic or hygroscopic material can be pre-soaked so that both the liquid absorbed by the hydrophilic or hygroscopic material and the liquid in the reservoir 1122 can contribute to the humidification of gases in the gases flow path 1116.
  • the tape 1120c of Figure 6C also includes an embodiment of the internal liquid reservoir 1122.
  • the walls of hydrophilic or hygroscopic material of the tape 1120c surrounding the reservoir 1122 are thinner than those of the embodiment of Figure 6B .
  • Thinner walls of the tape 1120c can allow liquid from the reservoir 1122 to permeate the hydrophilic or hygroscopic material and vapor to transfer to the gases flow path 1116 more readily.
  • thicker walls as in the embodiment of Figure 6B , can provide more structural strength to the tape 1120b.
  • the liquid reservoir 1122 can be filled and/or refilled in various ways, for example, by injecting, pumping, or pouring liquid into the reservoir 1122.
  • a vacuum can be generated within the reservoir 1122 by liquid in the reservoir 1122 becoming vapor and passing through the tape 1120 into the gases flow path 1116. The vacuum can provide a pressure differential to allow for refilling of the reservoir 1122.
  • the reservoir 1122 can also or alternatively be refilled using a water or other liquid bag.
  • the humidified and/or heated gases flowing through the gases flow path 1116 exit the housing 1110 through the gases outlet 1114 and flow into and through the delivery tube 1130.
  • the delivery tube 1130 can also include one or more heating elements 1150.
  • the heating elements 1150 can heat and/or help maintain a temperature of the humidified gases flowing through the delivery tube 1130 to a patient.
  • the humidification system 1100 therefore can employ a two-stage heating process.
  • the humidifier 1102 can generate humidity at a reasonably or generally consistent absolute humidity level based on the amount of energy or power supplied to the heating elements 1140 of the humidifier 1102. Subsequently, the heating elements 1150 in the delivery tube 1130 can help maintain the temperature of the gases to deliver humidity to a patient at a reasonably or generally consistent relative humidity level.
  • vapor can be released from a hydrophilic embodiment of the tape 1120 passively and/or without requiring heat.
  • the heating elements 1140 therefore may not be required or included in the humidifier 1102.
  • a concentration gradient drives movement of the water or vapor from the hydrophilic material of the tape 1120 to the gases flow path 1116.
  • the humidification system 1100 can include a control system.
  • the humidification system 1100 can include a power source for supplying power to the heating elements 1140, 1150 and/or the control system.
  • the control system can control the power supplied to the heating elements 1140 to control the amount of heat provided by the heating elements 1140, which in turn controls or affects the amount of vapor released from the tape 1120.
  • the humidifier 1102 therefore provides for passive water vapor delivery and does not require active control of the vapor delivery.
  • the control system and/or power source can be external to the humidifier 1102 and/or the delivery tube 1130.
  • the control system and/or power source can be housing within or integrated into a single housing or component.
  • the control system and/or power source can be mounted to a surgical tower or an insufflator.
  • the control system and/or power source can be connected to and receive power from a wall outlet.
  • FIGs 7 and 8 illustrate an example embodiment of a humidification system 1200 including an inline humidifier 1202 according to the present disclosure.
  • the humidification system 1200 includes the inline humidifier 1202 and a delivery tube or conduit 1230.
  • the inline humidifier 1202 is generally disc-shaped or circular. However, other shapes are also possible, for example, quadrilateral, square, trapezoidal, parallelogram, or other shapes.
  • the inline humidifier 1202 advantageously allows the humidification system 1200 to have a smaller footprint than prior art humidification systems such as those shown in Figures 1 and 2 .
  • the inline humidifier 1202 includes a housing or cover 1210, a permeable wall or membrane 1220, a liquid reservoir 1224, a gases flow path 1216, and a heater.
  • the inline humidifier 1202 includes a heater plate 1240, and the housing 1210 entirely surrounds other components of the inline humidifier 1202, including the heater plate 1240.
  • the inline humidifier 1202 includes a base 1222 that is coupled to the housing 1210 and that acts as a heater.
  • the permeable wall 1220 is positioned between the housing 1210 and the base 1222 as shown.
  • the gases flow path 1216 is bordered by the housing 1210 and the permeable wall 1220
  • the liquid reservoir 1224 is bordered by the permeable wall 1220 and the base 1222.
  • the base 1222 can be made from or include a material that is hydrophobic or liquid impermeable to contain the liquid within the reservoir 1224 and that is thermally conductive such that the base 1222 can act as the heater.
  • the base 1222 can be made of a metal such as aluminium.
  • the base 1222 is made of a combination of thermally conductive materials, such that the base 1222 can act as a heater, and thermally insulating materials, to help control or limit heat loss to the surrounding environment or atmosphere.
  • Outer edges or perimeters of the housing 1210 and the base 1222 can be coupled together to encase the permeable wall 1220, the liquid reservoir 1224, and the gases flow path 1216.
  • the housing 1210 and the base 1222 can be coupled together via an adhesive, welding, crimping or bending the edges together, or any other suitable means.
  • the edges of the housing 1210, the base 1222, and the permeable wall 1220 can be folded or crimped together with the edges of the permeable wall 1220 sandwiched between the edges of the housing 1210 and the edges of the base 1222.
  • the inline humidifier 1202 has a gases inlet 1212 and a gases outlet 1214.
  • the gases inlet 1212 can be coupled directly to an insufflator outlet port or can be coupled to the insufflator outlet port via a supply tube or conduit.
  • the gases outlet 1214 is coupled to a first end of the delivery tube 1230 in use.
  • the delivery tube 1230 is permanently coupled to the gases outlet 1214.
  • the delivery tube 1230 can be removably coupled to the gases outlet 1214.
  • the delivery tube 1230 can be provided preassembled to the gases outlet 1214.
  • An opposite, second end 1234 of the delivery tube 1230 is coupled to a patient interface, for example, a laparoscopic cannula, or another humidification system component in use.
  • the humidification system 1200 is disposable. In other embodiments, the humidification system 1200 can be refillable and/or sterilisable for reuse.
  • the housing 1210 can be made of a hydrophobic or any other gases and/or water impermeable or low permeability material. In some embodiments, the housing 1210 includes insulation to reduce or minimize heat transfer with the external environment or atmosphere. As shown in Figures 9-10 , the gases inlet 1212 and the gases outlet 1214 can be disposed or formed in the housing 1210 on a rear side of the inline humidifier 1202.
  • the gases inlet 1212 can be disposed on a front side of the inline humidifier 1202 as shown in Figure 7 (e.g., disposed or formed in the base 1222 of Figure 10 or a front side of the housing 1210 of Figure 7 ) or on a side or edge of the inline humidifier 1202 (e.g., a side or edge of the housing 1210) and/or the gases outlet 1214 can be disposed on a front side of the inline humidifier 1202 or on a side or edge of the inline humidifier 1202 (e.g., on a side or edge of the housing 1210).
  • the gases inlet 1212 can be positioned proximate an outer perimeter of the inline humidifier 1202 or closer to the outer perimeter than a center of the inline humidifier 1202.
  • the gases outlet 1214 can be positioned at or proximate a center of the inline humidifier 1202.
  • the gases inlet 1212 can be positioned proximate the center of the inline humidifier 1202 and the gases outlet 1214 can be positioned proximate the outer perimeter of the inline humidifier 1202, both the gases inlet 1212 and the gases outlet 1214 can be positioned proximate the center of the inline humidifier 1202, both the gases inlet 1212 and the gases outlet 1214 can be positioned proximate the outer perimeter of the inline humidifier 1202, or the gases inlet 1212 and the gases outlet 1214 can be positioned at any position between the center and outer perimeter on either side of the inline humidifier 1202.
  • the permeable wall 1220 separates the liquid reservoir 1224 from the gases flow path 1216.
  • the permeable wall 1220 is permeable to vapor but is substantially impermeable to gases and liquid.
  • the permeable wall 1220 can be made of a polymer, fiber, paper, or other material.
  • the permeable wall 1220 can be made of a porous or non-porous material. If the permeable wall 1220 is made of a porous material, the cells of the porous material can be open or closed in different percentages. The percentage of open and closed cells of the porous material can be controlled by the void size and void fraction.
  • an outer layer of closed cells can be created in an otherwise open cell material by quickly cooling the outer surface of the material after extrusion.
  • the permeable wall 1220 can be made of a non-porous material such as Arnitel or Estane.
  • the permeable wall 1220 can be made of a porous material such as foamed Arnitel or foamed Estane.
  • the permeable wall 1220 can be made in the form of a film, mesh, web, or a foamed variant of a film, mesh, or web.
  • the permeable wall 1220 can include or be made of a hydrophilic, hygroscopic, or microporous material.
  • a hydrophilic material absorbs water in a vapor and/or liquid state.
  • a hydrophilic material can be foamed and/or can include surface features to increase the effective area of the material.
  • a microporous material e.g., Gore-Tex, is formed in such a way that a pore size of the material is small enough to prevent or inhibit liquid (e.g., water) from passing through but large enough to allow vapor (e.g., water vapor) to pass through.
  • the permeable wall 1220 can be thin and designed to have a high surface area in contact with the liquid in the reservoir 1224 and the gases in the gases flow path 1216 to improve or optimize exchange of vapor into the gases.
  • the permeable wall 1220 can have surface features to increase the effective surface area of the hydrophilic, hygroscopic, or microporous material. Such surface features can be positioned on either or both sides (i.e., the side in contact with the gases flow path 1216 and/or the side in contact with the liquid reservoir 1224) of the permeable wall 1220.
  • the permeable wall 1220 can have a textured finish, such as, for example, a finish resembling sandpaper.
  • the permeable wall 1220 can have a pattern of protrusions, microstructures, and/or microchannels.
  • the surface features can be applied to the permeable wall 1220 after extrusion or other processing of the material or can be formed integrally with the permeable wall 1220 during extrusion or other processing.
  • the reservoir 1224 When prepared for use, the reservoir 1224 contains a liquid such as water.
  • the reservoir 1224 is in thermal communication with the base 1222 or the heater 1240.
  • power is provided to the base 1222 or the heater 1240, and heat from the base 1222 or the heater 1240 heats the liquid in the reservoir 1224 to create vapor.
  • the vapor then passes through the permeable wall 1220 to the gases flow path 1216, where the vapor humidifies gases flowing through the gases flow path 1216.
  • the base 1222 or the heater 1240 can be a resistance heater and can allow for improved or optimum transfer of energy into the reservoir 1224.
  • a wall 1218 within the inline humidifier 1202 defines the gases flow path 1216 extending between the inlet 1212 and the outlet 1214.
  • the wall 1218 can be coupled to or integrally formed with an inside surface of the housing 1210 as shown in Figures 10-11 .
  • the wall 1218 can extend from, be coupled to, or be integrally formed with the permeable wall 1220.
  • the wall 1218 can be formed by a separate insert disposed between the permeable wall 1220 and the housing 1210.
  • the wall 1218 is formed in a spiral to define a spiral arrangement of the gases flow path 1216. Other arrangements for the wall 1218 and the gases flow path 1216 are also possible.
  • the wall 1218 extends perpendicularly from the rear side or surface of the housing 1210 and has a rectangular cross-sectional shape. In other embodiments, the wall 1218 can extend (from the housing 1210, from the permeable wall 1220, or as an insert separate from the permeable wall 1220 and/or the housing 1210) at an angle other than 90° relative to the rear side or surface of the housing 1210.
  • the wall 1218 can have a cross-sectional shape other than rectangular.
  • the inlet 1212 is positioned proximate the outer perimeter of the housing 1210
  • the outlet 1214 is positioned proximate the center of the housing 1210
  • the gases flow path 1216 follows a spiral path from an outer perimeter of the housing 1210 to a center of the housing 1210.
  • gases in the gases flow path 1216 become warmer as the gases travel inward toward the center of the housing 1210 and to the outlet 1214, and the gases are insulated by gases in portions of the gases flow path 1216 disposed concentrically outward.
  • the gases flow path 1216 instead followed a path from the center of the housing 1210 to the perimeter of the housing 1210, the warmest gases at the end of the gases flow path 1216 and at the outlet 1214 would be at the outer perimeter of the housing 1210 and therefore less insulated, which could reduce the efficiency of the system.
  • a spiral arrangement of the gases flow path 1216 can advantageously reduce or minimize flow dead spots in which the flow of gases recirculates or slows and/or can help minimize pressure losses.
  • a gases flow path having corners and features around which the gases must flow can cause resistance to flow and increase the pressure drop through the humidifier 1202.
  • the humidification system 1200 or the humidifier 1202 can be supplied sterilized and ready for use.
  • the humidification system 1200 specifically the reservoir 1224, can be prefilled (e.g., during manufacturing and assembly or set-up) with a volume of liquid, such as water, prior to a surgical procedure or other use.
  • the reservoir 1224 can be sized to hold a volume of liquid sufficient for an average duration of a typical procedure (e.g., a laparoscopic procedure or open procedure) for which the humidification system 1200 is intended to be used.
  • the humidification system 1200 therefore does not require a separate liquid reservoir or delivery system outside of the humidifier 1202, and medical personnel need not input liquid into the system prior to use during set-up.
  • the humidifier 1202 can be refilled after use for re-use or during use if needed.
  • Power is supplied to the base 1222 or the heater 1240 such that the base 1222 or the heater 1240 heats the liquid stored in the reservoir 1224 to form vapor that can then pass through the permeable wall 1220 into the gases flow path 1216. Gases flowing through the gases flow path 1216 are therefore humidified by the vapor passing through the permeable wall 1220.
  • the heated vapor can also heat the gases flowing through the gases flow path 1216.
  • the hydrophobic, impermeable, or low permeability material of the housing 1210 can help hold the vapor within the housing 1210 and prevent or inhibit the vapor from being released through the housing 1210 to the atmosphere.
  • the liquid reservoir 1224 can be filled and/or refilled in various ways, for example, by injecting, pumping, or pouring liquid into the reservoir 1224.
  • a vacuum can be generated within the reservoir 1224 by liquid in the reservoir 1224 becoming vapor and passing through the permeable wall 1220 into the gases flow path 1216. The vacuum can provide a pressure differential to allow for refilling of the reservoir 1224.
  • the reservoir 1224 can also or alternatively be refilled using a water or other liquid bag.
  • the reservoir 1224 is detachable from the humidifier 1202 such that the reservoir 1224 can be refilled and/or replaced.
  • the humidifier 1202 or the humidification system 1200 can include a supplemental liquid storage section.
  • a supplemental liquid storage section can provide additional liquid storage and supply in addition to the liquid stored in the liquid reservoir 1224.
  • only the reservoir 1224 is in contact with the permeable wall 1220.
  • the reservoir 1224 and the supplemental liquid storage section can be connected such that liquid can pass between the reservoir 1224 and the supplemental liquid storage section.
  • a supplemental liquid storage section is connected to the reservoir 1224 via a connector, such as a tube, that allows liquid to flow between the reservoir 1224 and the supplemental storage section.
  • the connector can be sized such that a flow rate between the supplemental storage section and the reservoir 1224 is greater than, but close to, a rate of vapor transfer through the permeable wall 1220.
  • Liquid can be transferred from the supplemental storage section to the reservoir 1224 via gravity, active means such as a pump, and/or passive means such as a wicking material.
  • the reservoir 1224 and/or the supplemental storage section can be detachable from the humidifier 1202 and may therefore be replaceable.
  • the reservoir 1224 and/or the supplemental storage section are integrally formed or permanently coupled to or disposed within the humidifier 1202.
  • the reservoir 1224 and/or the supplemental storage section can be sealed and not refillable.
  • the reservoir 1224 and/or the supplemental storage section can be refillable with the use of specialized tools and/or a specialized process. Requiring specialized tools and/or a specialized process can restrict the ability of unqualified individuals to tamper with the reservoir 1224 and/or the supplemental storage section.
  • the reservoir 1224 and/or the supplemental storage section has an opening through which the reservoir 1224 and/or the supplemental storage section can be filled or refilled.
  • the opening can be covered and sealed (either temporarily such that the reservoir and/or supplemental storage section can be refilled or permanently after initial manufacturing and assembly) with a lid, cap, or other sealing apparatus to seal the reservoir 1224 and/or the supplemental storage section from the external environment.
  • the seal can be gas and/or liquid tight. If the reservoir 1224 and/or the supplemental storage section are sealed in a gas tight manner, the reservoir 1224 and/or the supplemental storage section can include a bleed valve (not shown).
  • the bleed valve allows air into the reservoir 1224 and/or the supplemental storage section to help equalize pressure within the reservoir 1224 and/or the supplemental storage section with the pressure of the external environment.
  • at least a portion of the permeable wall 1220 can be gases permeable and can act as a bleed valve to allow gases from the gases flow path 1216 to pass through the portion of the permeable wall 1220 into the reservoir 1224 and/or the supplemental storage section to help equalize the pressure.
  • the humidified and/or heated gases flowing through the gases flow path 1216 exit the housing 1210 through the gases outlet 1214 and flow into and through the delivery tube 1230.
  • the delivery tube 1230 can also include one or more heating elements 1250.
  • the heating elements 1250 can heat and/or help maintain a temperature of the humidified gases flowing through the delivery tube 1230 to a patient.
  • the humidification system 1200 therefore can employ a two-stage heating process.
  • the humidifier 1202 can generate humidity at a reasonably or generally consistent absolute humidity level based on the amount of energy or power supplied to the base 1222 or the heater plate 1240.
  • the heating elements 1250 in the delivery tube 1230 can help maintain the temperature of the gases to deliver humidity to a patient at a reasonably or generally consistent relative humidity level.
  • vapor can pass through a hydrophilic embodiment of the permeable wall 1220 passively and/or without requiring heat.
  • the heater plate 1240 therefore may not be required or included in the humidifier 1202, or the base 1222 may not need to act as a heater.
  • a concentration gradient drives movement of the water or vapor across the permeable wall 1220 to the gases flow path 1216.
  • the humidification system 1200 can include a control system.
  • the humidification system 1200 can include a power source for supplying power to the base 1222, the heater plate 1240, the heating elements 1250, and/or the control system.
  • the control system can control the power supplied to the base 1222 or the heater plate 1240 to control the amount of heat provided by the base 1222 or the heater plate 1240, which in turn controls or affects the amount of vapor that is formed and passes through the permeable wall 1220 to the gases flow path 1216.
  • the humidifier 1202 can therefore provide for passive water vapor delivery and does not require active control of the vapor delivery.
  • the control system can also or alternatively control the power supplied to the heating elements 1250 to control or affect a temperature of gases flowing in the delivery tube 1230 and delivered to a patient.
  • the control system and/or power source can be external to the humidifier 1202 and/or the delivery tube 1230.
  • the control system and/or power source can be housed within or integrated into a single housing or component.
  • the control system and/or power source can be mounted to a surgical tower or an insufflator.
  • the control system and/or power source can be connected to and receive power from a wall outlet.
  • FIGS 12 and 13 illustrate another example embodiment of a humidification system 1300 including an inline humidifier 1302 according to the present disclosure.
  • the humidifier 1302 includes a housing 1310 having an inlet 1312 and an outlet 1314, a heater 1340, and a permeable tube 1320.
  • the permeable tube 1320 is disposed in a spiral, although other configurations are also possible.
  • the permeable tube 1320 can define or surround a liquid reservoir therein, and a gases flow path can be defined around the permeable tube 1320 between the inlet 1312 and the outlet 1314.
  • the permeable tube 1320 can be in thermal communication with the heater 1340.
  • power can be supplied to the heater 1340 to heat the liquid within the tube 1320 to form vapor, and the vapor can pass through the permeable wall of the tube 1320 into the gases flow path.
  • the permeable tube 1320 can define or surround the gases flow path, and the permeable tube 1320 can be disposed in a liquid reservoir within the housing 1310 in thermal communication with the heater 1340.
  • power can be supplied to the heater 1340 to heat the liquid in the reservoir to form vapor, and the vapor can pass through the permeable wall of the tube 1320 into the gases flow path within the tube 1320.
  • the humidification system 1300 can include a control system and/or power source and/or can share other features described herein with respect to the humidification system 1100 and the humidification system 1200.
  • permeable materials including but not limited to permeable walls and membranes, should be understood to include materials that generally allow the passage or diffusion of vapour, but generally inhibit the passage or diffusion of liquid and gases, through the material. Such materials can also be referred to as breathable materials.
  • the apparatus and system of the disclosure may also be said broadly to consist in the parts, elements and features referred to or indicated in the specification of the application, individually or collectively, in any or all combinations of two or more of said parts, elements or features.
  • each embodiment of this invention may comprise, additional to its essential features described herein, one or more features as described herein from each other embodiment of the invention disclosed herein.
  • the terms “generally parallel” and “substantially parallel” refer to a value, amount, or characteristic that departs from exactly parallel by less than or equal to 15 degrees, 10 degrees, 5 degrees, 3 degrees, 1 degree, 0.1 degree, or otherwise.
  • a humidifier comprising: an inlet and an outlet and a gases flow path extending from the inlet to the outlet; a liquid reservoir in thermal communication with, or configured to be in thermal communication with in use, a heater; and a permeable wall separating the liquid reservoir from the gases flow path; wherein, in use, the heater heats liquid stored in the liquid reservoir to form vapour, and the vapour passes through the permeable wall to humidify gases in the gases flow path.
  • the reservoir is configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidifier.
  • the gases flow path is defined by a spirally wound wall within the housing.
  • the humidifier comprises a hydrophobic housing.
  • the permeable wall comprises a tape.
  • a humidifier comprising: a housing having an inlet and an outlet; and a tape disposed within the housing and at least partially defining a gases flow path through the housing between the inlet and the outlet, wherein the tape comprises a hydrophilic material configured to hold a volume of liquid and a heating mechanism configured to heat liquid held within the hydrophilic material to produce vapour.
  • the hydrophilic material is configured to hold sufficient liquid to produce vapour for an intended volume of gases passing through the humidifier.
  • the hydrophilic material is configured to be pre-loaded prior to use to cause liquid to be held within the hydrophilic material.
  • the tape is spirally wound within the housing.
  • the housing comprises a hydrophobic material.
  • the heating mechanism comprises at least one heater wire disposed within and surrounded by the hydrophilic material.
  • the delivery tube comprises a second heater or heating mechanism.
  • the second heater or heating mechanism comprises at least one heater wire disposed within the delivery tube.

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  • Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pulmonology (AREA)
  • Emergency Medicine (AREA)
  • Air Humidification (AREA)
EP23189049.2A 2016-01-21 2017-01-20 System zur befeuchtung von medizinischen gasen Pending EP4282458A3 (de)

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US201662281632P 2016-01-21 2016-01-21
US201662281612P 2016-01-21 2016-01-21
EP17741725.0A EP3405246B1 (de) 2016-01-21 2017-01-20 System zur befeuchtung von medizinischen gasen
PCT/NZ2017/050005 WO2017126982A1 (en) 2016-01-21 2017-01-20 System for humidification of medical gases

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WO2017179569A1 (ja) * 2016-04-13 2017-10-19 株式会社メトラン 加湿器、呼吸補助装置

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EP3405246A1 (de) 2018-11-28
AU2017208699B2 (en) 2022-02-03
EP3405246B1 (de) 2023-08-09
US20210370012A9 (en) 2021-12-02
AU2017208699A1 (en) 2018-08-02
AU2022202923A1 (en) 2022-06-02
US11207487B2 (en) 2021-12-28
EP3405246A4 (de) 2019-08-28
EP4282458A9 (de) 2024-02-14
US20210077768A1 (en) 2021-03-18
US20220134045A1 (en) 2022-05-05
AU2022202923B2 (en) 2024-03-07
CA3012036A1 (en) 2017-07-27
EP4282458A3 (de) 2024-02-21
WO2017126982A1 (en) 2017-07-27

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